William Newman
Impact in
- Genetics top 0.1%
- Inflammatory Bowel Disease
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Immunology top 0.5%
- Immune Cell Function and Interaction
- IL-33, ST2, and ILC Pathways
Papers in
- Genetics 121
- BRCA gene mutations in cancer 52
- Genomics and Rare Diseases 27
- Genetic Associations and Epidemiology 19
- Genomic variations and chromosomal abnormalities 17
- Pharmacology 30
- Pharmacogenetics and Drug Metabolism 30
- Co-authors
- D. Gareth Evans (44 shared papers)Katherine A. Payne (22 shared papers)Steve Roberts (19 shared papers)Helen Byers (23 shared papers)Miriam J. Smith (17 shared papers)Ajith Kumar Siriwardena (4 shared papers)Melissa Oliveira‐Cunha (2 shared papers)Jill E. Urquhart (17 shared papers)
- Journals
- The American Journal of Human Genetics (25 papers)Clinical Genetics (12 papers)Journal of Medical Genetics (8 papers)European Journal of Medical Genetics (8 papers)European Journal of Human Genetics (7 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
William Newman
313 papers receiving 19.1k citations
William Newman's Hit Papers
Peers
Comparison fields: 5 of 186
- Genetics 7.3k
- Immunology 3.2k
- Molecular Biology 6.6k
- Cancer Research 1.3k
- Gastroenterology 477
Countries citing papers authored by William Newman
This map shows the geographic impact of William Newman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by William Newman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William Newman more than expected).
Fields of papers citing papers by William Newman
This network shows the impact of papers produced by William Newman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by William Newman. The network helps show where William Newman may publish in the future.
Co-authors
The 25 scholars most cited alongside William Newman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 335 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease Hit paper breakdown → | 2012 | 3907 |
| 2 | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci Hit paper breakdown → | 2010 | 2123 |
| 3 | Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 Hit paper breakdown → | 2011 | 1139 |
| 4 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes Hit paper breakdown → | 2018 | 765 |
| 5 | 2009 | 457 | |
| 6 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 395 |
| 7 | 2007 | 339 | |
| 8 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses Hit paper breakdown → | 2020 | 303 |
| 9 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 10 | 2014 | 224 | |
| 11 | 2015 | 209 | |
| 12 | 2017 | 207 | |
| 13 | 2013 | 204 | |
| 14 | 2013 | 198 | |
| 15 | 2019 | 172 | |
| 16 | 2018 | 171 | |
| 17 | 2008 | 169 | |
| 18 | 2015 | 168 | |
| 19 | 1996 | 167 | |
| 20 | Recommendations for clinical interpretation of variants found in non-coding regions of the genome Hit paper breakdown → | 2022 | 165 |
About William Newman
William Newman is a scholar working on Genetics, Pharmacology, Molecular Biology, Urology and Cancer Research, having authored 335 papers that have together received 19.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (52 papers), Pharmacogenetics and Drug Metabolism (30 papers), Genomics and Rare Diseases (27 papers), RNA modifications and cancer (27 papers), Genetic Associations and Epidemiology (19 papers), Mitochondrial Function and Pathology (18 papers), Genomic variations and chromosomal abnormalities (17 papers) and Cancer Genomics and Diagnostics (16 papers). The work is most often cited by research in Genetics (7.3k citations), Immunology (3.2k citations), Molecular Biology (6.6k citations), Cancer Research (1.3k citations) and Gastroenterology (477 citations). William Newman has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include D. Gareth Evans, Katherine A. Payne, Steve Roberts, Helen Byers, Miriam J. Smith, Ajith Kumar Siriwardena, Melissa Oliveira‐Cunha, Jill E. Urquhart, Anthony Howell and Siddharth Banka. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Journal of Medical Genetics, European Journal of Medical Genetics and European Journal of Human Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.